|Publication number||US4064882 A|
|Application number||US 05/607,231|
|Publication date||Dec 27, 1977|
|Filing date||Aug 25, 1975|
|Priority date||Aug 25, 1975|
|Publication number||05607231, 607231, US 4064882 A, US 4064882A, US-A-4064882, US4064882 A, US4064882A|
|Inventors||George Michael Johnson, Kenneth Keith Krueger, Todor Pavlov|
|Original Assignee||Shiley Laboratories, Inc.|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (9), Referenced by (49), Classifications (9), Legal Events (3)|
|External Links: USPTO, USPTO Assignment, Espacenet|
Application Ser. No. 607,265, filed concurrently herewith, entitled RELIEF VALVE; Design Patent Application Ser. No. 607,264, filed concurrently herewith, entitled VALVE DESIGN.
This invention relates to tracheostomy tube design and particularly to improvements in the design of tracheostomy tube systems.
In a broader aspect, this invention relates to retention catheters, and other implements in which a retention or sealing balloon or like member is included.
Tracheostomy tubes of the type generally under consideration here maybe of the type illustrated in U.S. Pat. No. 3,659,612, to Donald P. Shiley. In its broader aspect, the invention is applicable to catheters generally of the type illustrated in U.S. Pat. No. 2,473,742, to Auzin, and similar devices.
The use of inflatable cuffs or balloons, or like members, to retain cannula in various body passages, for cleaning body passages, and for other purposes has long been known. The problem of providing an adequate inflation to the cuff, which is not visible during use, without over-inflating the cuff has plagued the surgical, medical and the medical implement arts for decades. Several approaches have been tried to obviate these problems. For example, the use of a balloon external to the patient connected by a fluid conductor to the inflatable cuff or balloon on the cannula is a common expedient which has been widely used. Often, the surgeon was required to make a visual estimate as to the degree of inflation of the internal cuff by looking at the external cuff. The visual indication may be valid in some instances but is unreliable and depends to a considerable extent upon the experience, skill and judgment of the user. In addition, since catheters, cannula of various kinds, and the balloons attached thereto are made of various materials, visual observations must be related to the materials being used to be valid. Consequently, the doctor had to use the same type of catheter or cannula previously used in order to have any degree of confidence in his estimation of the inflation of the retention balloon. More recently efforts have been made to provide automatic devices to prevent increased in-pressure in the retention cuff or balloon above a predetermined pressure. For example, in the McGinnis U.S. Pat. No. 3,642,005, there is disclosed an indicator type balloon which has an elastic wall formed of a material which continues to stretch without further increase in air pressure as additional air is injected into the system, thus the external balloon continues to stretch without increasing the pressure in the overall system and in the inflated cuff inside the body.
The present invention is an improvement in systems for preventing the over-inflation of retention ballons, cuffs, and the like devices on cannula, and other indwelling and temporary use medical and other implements.
One of the features of the invention is that the system can be compact and inexpensively made, with high reliability.
Another feature of the invention is that the system is less dependent upon the stretch characteristics of materials than devices in the prior art and, consequently, is more stable over long periods of storage, through sterilization cycles, and the like which tend to change the elastic characteristics of most materials.
A very important feature of this invention resides in the design and operation of the pressure relief valve component and the advantages characteristic to the valve.
In brief summary, this invention comprises a cannula having a retention cuff in fluid communication with a valve body which has a fluid inlet and a fluid outlet connected to each other through means forming a main passage through the valve. The main passage of the valve is normally closed by a main valve which is disposed and located in the main fluid passage. A vent passage system is provided in the valve in fluid communication with the main passage and with the exterior of the valve body, or to some other venting system. The vent system includes a vent valve normally closing the vent passage. The vent valve comprises a flexible valving member so constructed and disposed as automatically to open the vent passage when the pressure in the main passage applied through the vent passage and on the flexible valve member reaches a predetermined value. Once the vent passage is opened, fluid escapes from the main passage through the vent passage and past the vent valve thereby reducing the pressure applied through the main passage of the valve and preventing fluid pressure of greater than the predetermined value from being applied at the outlet of the main fluid passage.
There are many important and many convenient structural and functional features and relationships which will be apparent from the specification and the drawings.
FIG. 1 illustrates a tracheostomy tube assembly of this invention finds particular utility.
FIG. 2 depicts the improved valve which is an important aspect of this invention with its components in exploded isometric view.
FIG. 3 depicts the valve in cross-section having a luer tip inserted therein and the main valve in open position.
The major components of the tracheostomy system which is the exemplary and illustrative embodiment of the overall invention described herein include the pressure relief valve 10, which will be described in complete detail hereinafter, the indicator balloon 30, the tracheostomy cannula 40, including the retention cuff 50 connected by a fluid conduit 60 to the indicator balloon and the pressure relief valve. Pressure is conventionally applied by means of a syringe, however, any other pressure applying means may be used.
It will be understood that the illustrative embodiment exemplifies only one preferred form of the invention and that, in lieu of the tracheostomy tube, balloon or cuff equipped cannula generally such as embolectomy catheters, indwelling catheters, ureteral chatheters and the like, and other devices which are equipped with inflatable cuffs, balloons or other elements which are inflated in the body or in other locations where they are not visible may be used in connection with the present invention.
The tracheostomy tube including the cuff and the indicator balloon may, in the exemplary form of the invention, be of the type described in the aforesaid patent of Donald P. Shiley.
With reference to the figures generally, the valve 10 comprises an inlet member 12 having an opening 14 adapted to receive luer adapter inlet 16, and an outlet member 18. The valve also includes a main valving member 20 received in a main passage of the valve, a flow restriction and air filter 21 between the main valve member 20 and the inlet, a spring 22 biasing the main valve to the normally closed position, and a vent valve assembly which includes a diaphragm 24, a washer 26 and a spring 28 which biases the washer and the diaphragm to the normally closed position.
It will be apparent from the general description that there are many ways of constructing and assemblying the valve. It will also be apparent that various equivalent structures, elements, and means may be used to accomplish the same functions in substantially the same way. For example, while a compression spring is illustrated as the biasing means for both of the main valves and the vent valve, their biasing means generally would be equivalent. In addition, while a flat, annular diaphragm is illustrated, other flexible means would perform and function in an equivalent manner in the same or equivalent structural and functional combination. The best mode of making and using the invention presently known to the inventors is described as the preferred embodiment; however, the invention is not limited to the preferred embodiment, which is described in considerable detail to exemplify and illustrate the best mode for carrying out the invention and not in any respect for limiting the invention thereto.
In the exemplary, illustrative embodiment shown in the drawings, the inlet member is generally circular in configuration since this provides aesthetically advantageous features as well as functional efficiency. Adjacent the periphery 100 and spaced slightly inwardly is an annular ridge 102 which is adapted to be received in a groove in the outlet member, which will be described in detail hereinafter, during assembly of the valve. On the inside of the inlet member, adjacent the rib 102 and spaced slightly inwardly therefrom is a raised peripheral ridge 104 which cooperates with a ridge on the outlet member, which will be described hereinafter in detail, for sealing therebetween the diaphragm 24. The surface 106 is annular in configuration and defines the space between the diaphragm sealing ridge 104 and a valve seat ridge 108 which is interior to and, in the preferred embodiment, concentric with the diaphragm sealing ridge 104.
Also concentric with the diaphragm sealing ridge 104, in the preferred embodiment, and interior of the ridge 108 is a tubular main fluid conductor extension 110 which forms therethrough the main fluid passage 112, in which is loosely received the valve member 20.
On the other side of the inlet member 12 there is formed the opening 14 for receiving the luer tip adapter 16. In the preferred embodiment, the luer tip opening is generally circular in configuration as indicated at 116 with side openings 118 and 118a having rounded ends 120 and 120a and the luer tip adapter is of similar size and configuration for being received and adhesively secured therein. Of course, the luer tip adapter and the inlet member may be fashioned of more than two pieces or of less than two pieces, depending upon the manufacturing technique desired. The luer tip adapter has a luer inlet 122 which is adapted to receive a luer, indicated at 124, tightly therein to permit fluid communication from the interior of the syringe to the main passage, as will be described hereinafter. The inlet 122 widens at a shoulder 128 to a larger inlet passage 130. The restriction 21 is adapted to be received in the enlarged inlet passage 130 adjacent the seat 128 formed by the juncture of inlet passage portions 122 and 130. The flow restriction 21 may be simply a flat circular or other configuration porous disc or a porous plug of any other desired configuration depending upon the desired shape, size and configuration of the inlet passage and the valve element 20. The function of the restriction 21 will be described in more detail hereinafter.
In the preferred embodiment, the luer tip adapter 16 is so constructed and disposed in the opening as to provide a space forming a passage 132 extending outwardly from the passage 130 and in fluid communication with an opening 134 through the inlet member into an inlet portion of a chamber defined by the wall 106, the diaphragm 24, and the ridges 104 and 108, all of which are in the vent passage system as will be described hereinafter.
The outlet member 18 is, in the preferred embodiment, likewise circular in configuration for aesthetic purposes which are consistent with the efficiency of material use and functional characteristics. Slightly inwardly of the periphery 140 is a groove 142 which receives the ridge 102 of the inlet member. In the preferred method of assembly, the ridge 102 and the groove 142 are ultrasonically welded together, after the diaphragm, washer, etc. are properly positioned in place. Still further inwardly of the periphery 140 and the groove 142 is a ridge 144 which is annular in configuration and constructed and adapted to cooperate with the diaphragm sealing ridge 104 on the inlet member to secure and seal therebetween the edge of the diaphragm 24. The diaphragm 24 may be held in position by the compressive force applied betwen the diaphragm sealing edges 104 and 144 or by adhesive applied between the ridges 104 and 144 and the diaphragm 24, or by a combination of compressive and adhesive securement, or by other means. An annular tubular portion 148 forms a main passage portion 150 which, in the preferred embodiment, is generally co-axial with the main passage portion in the inlet member. The outlet member also forms a valve seat 152. In the preferred embodiment, the annular tubular portion forming the main passage portion in the outlet member is constructed and adapted to mate with the conductor extension forming the main passage portion of the inlet member so as to connect to two main passage portions into a single main passage separate from the chamber which surrounds the main passage. In the preferred embodiment, this mating is in the form of a shoulder joint 154 between the distal end of the annular tubular portion of the outlet member and the conductor extension of the inlet member. A fluid tight mating seal may be formed by precision contact, a compression sealing member such as an O-ring or washer, or by adhesively securing the two elements together, as may be preferred in any particular assembly method.
An annular chamber portion 156 is formed between the annular tubular portion 148 and the wall 158 of the outlet member, the function of which will be described in detail hereinafter.
The outlet includes an outlet opening 160, the juncture between the passage 150 and the outlet opening 160 forming an annular shoulder 162, the function of which will also be described later. One or more vent openings 164 are provided fluid to permit communication from exterior of the valve body, or to some other venting means, and the vent chamber defined by the wall of the outlet member, the diaphragm 24, rib 144, and by combination of the conductor extension 110, the tubular portion 148 and the wall 158. This outlet chamber forms a part of the vent system as will be described hereinafter.
The valve element 20 is generally cylindrical in nature having an elongate cylindrical portion 170 extending loosely through and in spaced relationship with respect to the walls of the main passage portion 112 and into the inlet passage portion 130. The valve also includes an enlarged cylindrical portion 172 joined with the cylindrical portion 170 by a beveled or tapered face 174, the latter forming a valve surface for contact with the valve seat 152. In the preferred embodiment, a short boss 176 extends on the other side of the shoulder 172 for receiving and positioning the compression spring 22 which is held in compression between the valve 20 and the shoulder 162 to provide resilient biasing of the valve 20 into the closed position, with the seat 152 and the valving surface 174 in contact. In the preferred embodiment, the extension 170 is generally cylindrical in configuration although a slightly frusto-conical configuration may be slightly advantageous in providing freedom of movement.
In the preferred embodiment, the diaphragm 24 is simply an annular flexible member having an outer circumferential portion 190 secured between the ribs 104 and 144 as previously described and an inner annular circumferential portion 192 received around the conductor extension of the inlet member and spaced therefrom slightly to permit fluid flow between the diaphragm and the conductor extension as part of the vent passage system. It is desirable to provide an annular washer 26 which has a generally flat outer annular portion 200 extending from an inner annular sleeve 202 which surrounds the conductor extension in spaced relationship substantially in the manner described with respect to the inner circumferential portion 192 of the diaphragm. The washer 26 maintains the diaphragm in substantially flat configuration and provides a uniform surface for exerting a resilient closing force from the spring 28, which is received around the sleeve portion 202, against the annular portion 200 at one end and in the annular chamber portion 156 at the other end. The resilient force provided by the compression coil spring 28 is exerted through the washer 26 to the diaphragm 24 to an internal annular portion 194 adjacent the internal circumference 192. The contact between the annular valve portion 194 of the diaphragm 24 and the rib 108 of the inlet member 12 provides the vent valve action.
In operation, the valve outlet member is connected to a tracheostomy cuff, which requires that applied pressure not exceed a predetermined value.
Fluid pressure applying means, such as a nozzle connected through a fluid conduit to a source of pressurized or convenient fluid source, is inserted in the inlet. In describing the operation of the valve hereinafter, reference will be made to the use of a syringe with a luer tip for opening the main passage valve, but it will be understood that any other fluid pressure applying means can be used in an equivalent manner.
As the luer tip is inserted into the inlet, the tip contacts the restriction 21 through which the fluid is filtered.
If filtering is not required, the valve can be actuated directly.
In either event, the valve 20 would be moved away from the inlet, separating the valve face portion 174 from the valve seat 152, thereby opening the main valve and permitting fluid flow through the main passage of the valve from the inlet, through the main passage past the main valve to the outlet of the valve and into the cuff. Thus, the main passage system permits the application of pressurized fluid to a cuff upon insertion of the leur or other pressure applying means into the inlet.
In order to limit the pressure which is applied to the outlet of the valve and to the cuff to a predetermined value, a vent passage system including the passage 132 which is in communication with the main passage through an opening 134 into an inlet portion, defined by wall 106, diaphragm 24 and ribs 104 and 108 of a chamber surrounding the main passage. When the pressure applied against diaphragm 24 reaches the predetermined value, the diaphragm 24 is moved by the pressure on the diaphragm such that an annular valving portion 194 of the diaphragm is spaced from the valve seat ridge 108 to permit fluid flow through the valve, through the annular passage formed by the space between the diaphragm inner circumference 192 and the conductor extension 110, into the outlet portion of the chamber surrounding the main passage defined by the other side of the diaphragm 24, ridge 144, the conductor extension 110 and tubular portion 148, wall 158 and the wall portion 166 of the outlet member and through vent 164 outside of the valve body. Fluid will flow so long as the pressure in the main passage is above the predetermined value for opening the vent valve. The effect of opening the vent valve is to maintain the pressure in the main passage to substantially the predetermined value required to open the vent valve. The amount of gas flowing through the vent system will depend upon the level of pressure applied to the inlet of the valve, but the pressure applied at the outlet of the valve will remain at substantially the predetermined pressure required to open the vent valve within a broad range of pressures applied to the inlet.
It will be understood that the venting action of the valve may not be to the exterior of the actual body but simply into another venting or passage system which, of course, would be equivalent to venting outside the body as described herein.
The pressure required to open the vent valve may be predetermined by selecting compression spring 28 requiring the predetermined force to compress the spring. In addition, the diaphragm 24 may be made of a semi-rigid material, such as phosphor bronze, brass, or other spring-type material in which additional biasing means in the form of compression spring 28 would not be required, the normally closed position being attained by the natural configuration of the diaphragm. Other means for maintaining the vent valve in normally closed position, such as extention springs, resilient bodies, etc., connected to or bearing against the diaphragm may be provided as desired.
In the preferred embodiment the valve body is preferably injection molded of polypropylene, delrin, ABS resin, or other desired material and the diaphragm is preferably of neoprene, or other soft, resilient material. The springs may be fabricated of virtually any material, but are preferably of a non-corrosive material which is compatible, at least for short times, with body fluids, although this is not a requirement in many applications. Stainless steel springs or springs formed of various plastics, such as nylon, delrin, etc., may be used where biological inertness is desired.
One of the important features of the valve is that it prevents any reverse flow from the cuff through outlet of the valve through the main passage except when a pressure applying device, such as a syringe, is connected to the inlet. Another important feature is that the vent is connected only to the main passage between the main valve and the inlet so that the vent system and pressure controlling means therein becomes operational only when the fluid source, e.g. the luer tip, is in the inlet of the valve.
In the preferred embodiment, as illustrated, the vent valve and pressure regulating system includes a diaphragm in which the valving surface is near the center of the diaphragm, proximate the interior circumference of the annular diaphragm in the preferred embodiment. Of course, the diaphragm may be secured adjacent the interior circumference or other portions of the diaphragm with the valving action taking place near the exterior of the diaphragm or at other portions thereof.
The example given above in which the valve is used as part of an improved tracheostomy tube system is, of course, merely illustrative of a typical use. As described and claimed in our aforementioned patent application entitled RELIEF VALVE, the valve finds utility and application in many other systems, including medical apparatus such as usage in connection with retention balloons of all types. It will be apparent from the foregoing discussion and from the illustrations that there are many variations which can be made of the various elements, combinational and constructional features of the illustrative embodiment without departing from the spirit and scope of the invention as defined in the following claims.
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|U.S. Classification||128/207.15, 604/99.02|
|Cooperative Classification||A61M16/04, A61M16/0465, A61M16/0497, A61M16/044|
|European Classification||A61M16/04B2, A61M16/04|
|Oct 29, 1992||AS||Assignment|
Owner name: SORIN BIOMEDICAL INC., CALIFORNIA
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNOR:SHILEY INCORPORATED;REEL/FRAME:006289/0029
Effective date: 19920226
|Dec 22, 1992||AS||Assignment|
Owner name: TRACHEOSTOMY PRODUCTS, INC., CALIFORNIA
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNOR:SORIN BIOMEDICAL INC.;REEL/FRAME:006348/0886
Effective date: 19921216
|Jul 18, 1994||AS||Assignment|
Owner name: MALLINCKRODT MEDICAL, INC., MISSOURI
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:TRACHEOSTOMY PRODUCTS, INC.;REEL/FRAME:007061/0274
Effective date: 19940628